Canonical Allele Identifier: CA2038995836

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750961C= , CM000674.2:g.57750961C=	GRCh38
NC_000012.11:g.58144744C= , CM000674.1:g.58144744C=	GRCh37
NC_000012.10:g.56431011C=	NCBI36
NG_007484.2:g.6421G= , LRG_490:g.6421G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.484G= MANE Select	ENSP00000257904.5:p.Ala162=
ENST00000257904.10:c.484G=	ENSP00000257904.5:p.Ala162=
ENST00000312990.10:c.265-290G=	ENSP00000316889.6:n.265-290G=
ENST00000546489.5:c.262G=	ENSP00000447779.1:p.Ala88=
ENST00000547281.5:c.262G=	ENSP00000447274.1:p.Ala88=
ENST00000549606.5:c.-158+1214G=	ENSP00000447005.1:n.-158+1214G=
ENST00000550419.5:c.484G=	ENSP00000448098.1:p.Ala162=
ENST00000551706.1:n.850G=
ENST00000551800.5:c.262G=	ENSP00000449391.1:p.Ala88=
ENST00000551888.5:n.443-290G=
ENST00000552254.5:c.484G=	ENSP00000449179.1:p.Ala162=
ENST00000552388.1:c.484G=	ENSP00000448963.1:p.Ala162=
ENST00000553237.5:c.*123G=	ENSP00000448885.1:n.*123G=
NM_000075.3:c.484G=	NP_000066.1:p.Ala162=
NM_000075.4:c.484G= MANE Select	NP_000066.1:p.Ala162=